At a Glance
- Tasks: Lead post-approval strategies and manage regulatory dossiers for medicines.
- Company: Perrigo, a global leader in healthcare and compliance.
- Benefits: Competitive salary, leadership development, and a dynamic work environment.
- Other info: Collaborative culture with opportunities for career advancement.
- Why this job: Make a real impact on global healthcare while developing your leadership skills.
- Qualifications: Experience in regulatory affairs and strong leadership abilities.
The predicted salary is between 63000 - 77000 £ per year.
Perrigo seeks an experienced Manager of Regulatory Affairs Lifecycle Management for Medicines in London.
You will lead post-approval strategies, manage regulatory dossiers, and oversee cross-functional teams to ensure compliant, timely submissions across a global portfolio.
You will drive lifecycle changes, collaborate with Quality, Safety, Supply Chain and R&D, and uphold Perrigo's commitment to high standards of compliance while developing your leadership capabilities in a global environment.
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Medicines Regulatory Lifecycle Lead employer: Perrigouk
Perrigouk is an exceptional employer that values innovation and collaboration, providing a dynamic work environment in the heart of London. Employees benefit from competitive compensation packages, including bonuses and a company car, alongside opportunities for professional growth through training and development initiatives. With a strong focus on fostering client relationships and enhancing product knowledge, Perrigouk empowers its team to make a meaningful impact in the healthcare sector.
